Method for preparing porous carbon composite material by utilizing silk screen as framework
A composite material and porous carbon technology, applied in the field of porous materials, can solve the problems of application obstacles, complicated operation, low product utilization rate, etc., and achieve the effects of simplified production process, high efficiency and easy operation
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Embodiment 1
[0034] Embodiment 1, with nickel-chromium alloy screen as skeleton, surfactant F127 as the system of porogen, the step of preparing porous carbon composite material is as follows: 2g F127 is dispersed in 50g ethanol; Dissolved into 0.5g again Hydroxypropiophenone and 1.5g phenolic resin polymer were stirred at 28°C for 1 hour to obtain a sol, and then the sol was attached to an area of 0.2m 2 , 200-mesh nickel-chromium alloy wire mesh. , and allowed the solvent to evaporate at 28°C for 10 hours. The resulting screen was placed in an oven at 120° C. for thermal polymerization treatment for 18 hours to obtain a composite material formed of F127 / polymer / screen. Then put the silk screen in a nitrogen-filled tube furnace and bake it at 630°C for 3 hours with a heating rate of 0.5°C / min to obtain a porous carbon composite material. Nitrogen adsorption and desorption isothermal tests show that the porous carbon composite has a mesopore diameter of 4.2nm and a pore volume of 0.08c...
Embodiment 2
[0035] Embodiment 2, with nylon screen as skeleton, nonionic surfactant F127 as porogen, the steps of synthesizing porous carbon composite material are as follows: 10g F127 is dispersed in 200g ethanol evenly; Then with 20g phenolic resin polymer Mix and stir at 25°C for 2 hours to obtain a sol; then attach the sol to an area of 1m 2 1. On a nylon screen with a mesh number of 200, the solvent was volatilized at 30° C. for 7 hours. The resulting screen was placed in an oven at 120° C. for aging for 24 hours to obtain a material formed of F127 / polymer / nylon screen. The screen was then placed in a tube furnace and roasted in nitrogen at 600°C for 3 hours at a heating rate of 0.5°C / min to remove the porogen and carbonize to obtain a porous carbon composite material. The nitrogen adsorption-desorption isotherm and pore size distribution show that the mesopore diameter is 4.1nm and the pore volume is 0.33cm 3 / g, the specific surface area is 550m 2 / g. The macropores are about...
Embodiment 3
[0036] Embodiment 3, with glass fiber network as skeleton, surfactant cetyltrimethylammonium bromide (CTAB) and F127 are as composite porogen, the step of synthesizing porous carbon composite material is as follows: 4.5gCTAB and 6g F127 Evenly dispersed in the mixed solution formed by 25g of methanol, then mixed with 7g of phenolic resin polymer, stirred at room temperature for 2 hours. 1 g of p-hydroxyamphetamine was then added, and the sol was obtained after continuous stirring at 40° C. for 100 minutes. The sol was then attached to an area of 1.5m 2 1. On a glass fiber net with a mesh number of 300, the solvent was evaporated at 30° C. for 5 hours. The obtained sponge was aged in an oven at 120° C. for 24 hours. A composite material formed by porogen / polymer / silk mesh is obtained. The glass fiber mesh was baked in a tube furnace with nitrogen flow at 650° C. for 3 hours with a heating rate of 0.5° C. / min to form a porous carbon composite material. The nitrogen adsorpt...
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